Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
  • C07C41/01—Preparation of ethers
  • C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups

Definitions

• This invention relates generally to the preparation of diaryl ethers or diaryl sulfides by a process involving a thoria-containing catalyst and more particularly con­cerns the use in such process of a catalyst comprising thoria deposited on neutral support particles.
• diphenyl ether-based monomers and diphenyl sulfide-based monomers are themselves potential useful monomers or can serve as precursors to monomers of proven utility such as oxybisanaline.
• 4,4′-diaminodiphenyl ether is currently used in the preparation of Torlon (R) and of Vespel (R) .
• Other diphenyl ether-based monomers which are of potential commercial importance include diacids, diols or dianhydrides of diphenyl ether.
• diphenyl ether-based monomers and diphenyl sulfide-based monomers have proven utility, their high cost and the lack of a convenient method of preparation have hindered any large volume applications of such monomers.
• a potentially inexpensive method of preparing diphenyl ether-based monomers and diphenyl sulfide-based monomers is the catalyzed dehydrative coupling of phenols or thiophenols, respectively.
• Unsupported and supported thorias have been employed as catalysts in the dehydrative coupling of phenols or thiophenols to form the correspond­ing diphenyl ethers of diphenyl sulfides, respectively.
• 911,246 discloses a method for the dehydrative coupling of a phenol to the corresponding diphenyl oxide in the presence of a catalyst containing thoria supported on alpha alumi­na, preferably in the vapor phase, and at substantially atmospheric pressure and at a temperature between 300°C and 550°C, for example, 475°C.
• the catalyst was prepared by impregnating alumina with thorium nitrate tetrahydrate and then decomposing the thorium nitrate to form thorium oxide.
• the patent states that, under conditions conducive to high catalyst activity in the dehydrative coupling reaction, the activity of the catalyst disclosed therein decreased with use. Furthermore, the data in the patent illustrates that the coupling reaction did not take place stereospecifically.
• thoria catalysts can also be prepared by the thermal decomposi­tion of thorium nitrate and thorium oxalate.
• the authors indicated that the results on catalysts prepared by these three different routes were comparable qualitatively.
• thoria catalysts for the production of certain, highly desirable stereospecific substituted diaryl ethers and diaryl sulfides are often less than is generally acceptable for a commercial pro­cess.
• thoria catalysts upon use under the conditions generally employed in the dehydrative coupling of phenols, thoria catalysts typically experience a significant loss of activity for such coupling reactions, with a further reduction in their selectivity for the production of certain, highly desirable stereospecific substituted diaryl ethers.
• a diaryl ether or a diaryl sulfide comprising heating a phenol, thiophenol, a ⁇ -hydroxy-­substituted fused aromatic ring-system compound, or a ⁇ -thio-substituted fused aromatic ring-system compound in the gas phase at a temperature in the range of from about 300°C to about 600°C in the presence of a bed of catalyst particles comprising thoria deposited on a neutral sup­port.
• Reactants that are suitable for use in the method of this invention are either a phenol, a thiophenol, a ⁇ -hydroxy-substituted fused aromatic ring-system compound, or a ⁇ -thio-substituted fused aromatic ring-system com­pound which, apart from the phenolic hydroxy or thio substituent in each thereof, is either otherwise unsubstituted or substituted either with at least one alkyl group containing from 1 to 10 carbon atoms, prefera­bly from 1 to 3 carbon atoms, or with at least one other substituent that is inert to the dehydrative coupling reaction, or with both thereof.
• each of the aforesaid optional alkyl substituent and other inert substituent is attached to an aromatic ring carbon atom that is attached to at least one aromatic ring carbon atom that is located other than ortho to the phenolic hydroxy or thio substituent.
• an aforesaid optional alkyl group substituent contains 3 or 4 carbon atoms and, in combination with an aromatic ring of the phenol, thiophenol or fused aromatic ring-system compound, forms a saturated ring fused to such aromatic ring.
• the reactant is a phenol or a ⁇ -hydroxy-substituted fused aromatic ring-system compound.
• suitable such materials include the following: phenol (diphenyl ether), ⁇ -naphthol (dinaphthyl ether), m-cresol (3,3′-dimethyldiphenyl ether), p-cresol (4,4′-dimethyldiphenyl ether), 3,4-xylenol (3,3′,4,4′-tetramethyldiphenyl ether), 3,5-xylenol (3,3′,5,5′-tetramethyldiphenyl ether), 3,4,5-trimethylphenol (3,3′,4,4′,5,5′-hexa­methyldiphenyl ether), 5-tetralinol (ditetralin ethers), and mixtures thereof such as m- and p-cresol (3,4′-dimethyldiphenyl ether).
• suitable feedstocks include compounds corresponding to the above-mentioned except that one or more methyl substituents therein are replaced by an ethyl or phenyl substituent, and/or the hydroxy substituent is replaced by a thio substituent.
• a catalyst suitable for use in the method of this invention comprises thoria deposited on a neutral support.
• a neutral support has no or very weak acidic or basic properties.
• Suitable neutral supports include pure silica, pure zirconia, carbon, asbestos, and quartz.
• the term "pure” means that the silica or zirconia contains less than 1000, preferably less than 500, parts per million of metallic impurities, calculated as the elemental metals.
• the support is fumed silica or fumed zirconia.
• fumed refers to the well-known method commonly used to prepare silica or zirconia. Fumed silica and fumed zirconia are commercially available for example, from the G. L. Cabot Company.
• the thoria content of the catalyst employed in the method of this invention is in the range of from about 1, preferably from about 10, to about 70 preferably to about 50 weight percent, calculated as ThO2 and based on the weight of the catalyst.
• the catalyst is prepared by direct calcination at 600°C-800°C of a suitable thorium salt impregnated by any convenient, conventional technique on the neutral support. Calcination at temperatures outside this range afforded catalysts of significantly lower activity.
• the support is calcined at 500°C-1000°C prior to being impregnated with the thorium salt.
• the aforesaid suitable thorium salt is typically impregnated on the neutral support by the incipient wetness method.
• Suitable thorium salts include the nitrate (tetrahydrate), carbonate, oxalate and hydroxide.
• the method of this invention is per­formed by passing the phenol, thiophenol, ⁇ -hydroxy-­substituted fused aromatic ring system compound or ⁇ -thio-substituted fused aromatic ring system compound in the vapor phase through a bed of particles of the afore­said catalyst at a weight hourly space velocity in the range of from about .01, preferably from about .1, to about 100, preferably to about 20, more preferably to about 5 grams of the feed compound per gram of the cata­lyst per hour.
• a solvent such as benzene, toluene, a xylene, a hexane, a heptane, tetrahydrofuran or 1,4-dioxane is used.
• the aforesaid phenol, thiophenol, ⁇ -­hydroxy-substituted fused aromatic ring-system compound, or ⁇ -thio-substituted fused aromatic ring-system compound is passed through the bed of aforesaid catalyst particles in the presence of a diluent gas which is substantially inert under the conditions employed in the method of this invention and which serves as a carrier gas to sweep the phenol, thiophenol, or ⁇ -hydroxy-substituted fused aromat­ic ring-system compound or ⁇ -thio-substituted fused aromatic ring-system compound through the catalyst bed.
• Suitable materials for this purpose include nitrogen, hydrogen and argon.
• hydrogen is employed. The use of hydrogen affords the additional advantage of increasing catalyst lifetime.
• the method of this invention is performed at a temperature in the range of from about 300°C, preferably from about 400°C, to about 600°C, preferably to about 500°C.
• a temperature in the range of from about 300°C, preferably from about 400°C, to about 600°C, preferably to about 500°C.
• reaction temperatures below 300°C little or no conversion of the reactant occurred.
• reaction tempera­tures above 600°C the formation of by-products was en­hanced, and selectivity for the formation of the desired product rapidly decreased.
• the catalyst undergoes deactivation on a long term basis, for example, losing about 38 percent of its initial activity over 10 days of operation. However, this deactivation can be overcome by a programmed increase in reaction temperature.
• the reaction temperature is gradually increased within the temperature range of from about 400°C, preferably from about 425°C, to about 500°C, preferably to about 450°C, at a rate of increase that is from about 0.04°C per day to about 0.45°C per day, preferivelyably to about 0.2°C per day, more preferably to about 0.085°C per day.
• a rate of increase that is from about 0.04°C per day to about 0.45°C per day, prefer strictlyably to about 0.2°C per day, more preferably to about 0.085°C per day.
• the method of this invention is performed at a pressure of from about 0.1 atmosphere, preferably from about 1 atmosphere to about 50 atmosphere, preferably to about 5 atmosphere.
• the resulting parti­cles impregnated with Th(NO3)2 ⁇ 4H2O were then dried overnight at 110°C and then calcined at 650°C for 12 hours.
• Example 1 The procedure of Example 1 was repeated, except that a neutral, fumed silica particle (Cabosil M-5 from J. L. Cabot Co.) (which had been mixed as a powder with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°C-1000°C for 12 hours and finally sieved) having a pore volume of 2.0 cubic centimeters per gram, as measured by water absorption, and being at least 99.99 weight percent pure and containing less than 2 parts per million by weight of aluminum and less than 5 percent per million by weight sodium, was employed instead of the fumed silica employed in Example 1.
• the resulting cata­lyst particles contained 42 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• Example 2 The procedure of Example 2 was repeated, except that a 28 weight percent concentration solution of Th(NO3)4 ⁇ 4H2O was employed instead of the solution con­taining 40 weight percent of Th(NO3)2 ⁇ 4H2O employed in Example 2.
• the resulting catalyst particles contained 27 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• Example 2 The procedure of Example 1 was repeated, except that 10 grams of 14/40-mesh acidic, relatively lower purity, (containing 300 parts per million by weight of aluminum and 800 parts per million by weight of sodium) colloidal silica particles (from Ludox Company) (which had been mixed as a powder with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°-1000°C for 12 hours and finally seived) containing 0.04 weight percent of alumina and having a pore volume of 1.5 cubic centimeters per gram, as measured by water adsorption, were used, instead of the fumed silica parti­cles employed therein.
• the resulting catalyst particles contained 23 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• Example 2 The procedure of Example 1 was repeated, except that 10 grams of 14/40-mesh, acidic, relatively lower purity, (only 99 weight percent pure and containing 1000 parts per million by weight of aluminum and 60 parts per million by weight of sodium) silicalite particles (which had been mixed as a powder with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°-1000°C for 12 hours and finally sieved) having a pore volume of 0.5 cubic centimeter per gram, as measured by water adsorption, were used instead of the fumed silica employed therein.
• the resulting catalyst particles contained 17 weight percent of thoria, calculated as ThO2 and based on the total weight of impregnated catalyst particles.
• Example 2 The procedure of Example 1 was repeated, except that 10 grams of 14/40-mesh neutral, zirconia particles (at 99.99 weight percent purity, containing less than 5 parts per million by weight of aluminum, solicon and sodium combined) (from Alrich Corporation) (which had been mixed as a powder with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°-1000°C for 12 hours and finally sieved) having a pore volume of 0.5 cubic centimeter per gram, as measured by water adsorption, were used, instead of the fumed silica particles employed therein.
• the resulting catalyst particles contained 16 weight percent of thoria, calculat­ed as ThO2 and based on the total weight of the impregnat­ed catalyst particles.
• Example 2 The procedure of Example 1 was repeated, except that 21.2 grams of an aqueous solution containing 50 weight percent of Th(NO3)4 ⁇ 4H2O and 27.7 grams of 14/42-mesh titanium oxide particles (at 99.5 weight percent purity, containing less than 0.3 weight percent of alumina) (P-25 from Degussa Corporation) (which had been mixed with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°C-1000°C for 12 hours) having a pore volume of 0.389 cubic centimeter per gram, as measured by water adsorption, were used instead of the solution and fumed silica particles employed therein.
• the resulting catalyst particlcs contained 15 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• Example 1 The procedure of Example 1 was repeated, except that 8.67 grams of an aqueous solution containing 54 weight percent of Th(NO3)4 ⁇ 4H2O. and 10.7 grams of 14/42-mesh basic magnesium oxide particles (at 98 weight percent purity, from Alpha Company) (which had been mixed with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°C-1000°C for 12 hours) having a pore volume of 0.343 cubic centimeter per gram, as measured by water adsorption, were used, instead of the solution and fumed silica particles employed therein.
• the resulting catalyst particles contained 17 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• Example 1 The procedure of Example 1 was repeated, except that 14.95 grams of an aqueous solution containing 50 weight percent of the Th(NO3)4 ⁇ 4H2O and 10.0 grams of 14/42-mesh fumed, acidic alumina particles (at about 99.6 weight percent purity, from Degussa) (which had been mixed with water to form a thick paste which was then dried overnight at 100°C and then calcined at 500°C-1000°C for 12 hours) having a pore volume of 0.68 cubic centimeter per gram, as measured by water adsorption, were used, instead of the solution and fumed silica particles employed therein.
• the resulting catalyst particles contained 30 weight percent of thoria, calculated as ThO2 and based on the total weight of the impregnated catalyst particles.
• ThO2 weight percent of thoria
• a variety of aluminas were similarly tested and shown to be ineffective in the coupling reac­tion of the method of the invention.
• Th(NO3)4 ⁇ 4H2O thorium nitrate
• Example 11-23 was performed using a simple quartz tube furnace reactor which had an inside diameter of 1.2 centimeters and was charged with 5 milliliters of 14/42-mesh catalysts which filled an 8-centimeter length of the reactor. The tube was then placed in a single zone 12-inch Lindberg furnace controlled by a Eurotherm 919 system. P-cresol was added at a general rate of 0.09-0.11 gram per minute using a Harvard Apparatus syringe drive. P-cresol was dissolved in toluene at a mole ratio at 1:1 of toluene-to-p-cresol prior to addition. Generally, nitrogen at a 10 milliliter per minute flow rate was passed through the reactor and catalyst bed.
• the contact time of the feed compound and the catalyst bed was 3-4 seconds.
• Long term catalyst deactivation runs were performed in a similar fashion except that reactants were added at a constant controlled rate using a Constametice Model I pump. Components of the product mixture were identified by gas chromatography or gas chromatography-mass spectometry. Major products were separated by recrystallization or distillation.
• Example 11-23 The catalysts and conditions employed in Example 11-23 are indicated in Table 1, and the results from such examples are indicated in Table 2.
• the use in Examples 11-13 and 15 of the acidic supports resulted in increased amounts of isomerization, dealkylation, alkylation, and hence, reduced selectivities for the formation of the desired product.

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• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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• 1987
  • 1987-11-16 US US07/121,151 patent/US4898982A/en not_active Expired - Fee Related
• 1988
  • 1988-11-11 EP EP19880310664 patent/EP0317208A3/de not_active Withdrawn
  • 1988-11-16 JP JP63289935A patent/JPH01165540A/ja active Pending

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